Syntaxin Binding Protein 1 (STXBP1)
[Edit]UNC18A; MUNC18-1; UNC18; hUNC18; p67; rbSec1; Protein unc-18 homolog 1
STXBP1 encodes a syntaxin-binding protein. The encoded protein appears to play a role in release of neurotransmitters via regulation of syntaxin, a transmembrane attachment protein receptor. Mutations in this gene have been associated with infantile epileptic encephalopathy-4. Alternatively spliced transcript variants have been described. predicted 68-kD n-Sec1 protein shares 27% identity with S. cerevisiae Sec1 and 59% identity with C. elegans Unc18. RNA blot analysis showed that n-Sec1 mRNA expression was neural-specific.The highest levels of expression were observed in retina and cerebellum. This mRNA contains an additional exon and encodes a predicted 603-amino acid protein. Two alternatively spliced forms of STXBP1 are also found in rat, and the predicted proteins are identical to their human counterparts.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Syntaxin Binding Protein 1 (STXBP1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Syntaxin Binding Protein 1 (STXBP1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Syntaxin Binding Protein 1 (STXBP1) | ELISA Kit Customized Service Offer |
Organism species: Mus musculus (Mouse)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Syntaxin Binding Protein 1 (STXBP1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Syntaxin Binding Protein 1 (STXBP1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Syntaxin Binding Protein 1 (STXBP1) | ELISA Kit Customized Service Offer |
Organism species: Rattus norvegicus (Rat)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Syntaxin Binding Protein 1 (STXBP1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Syntaxin Binding Protein 1 (STXBP1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Syntaxin Binding Protein 1 (STXBP1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Syntaxin Binding Protein 1 (STXBP1) | ELISA Kit Customized Service Offer |
- "A murine neural-specific homolog corrects cholinergic defects in Caenorhabditis elegans unc-18 mutants."J. Neurosci. 16:6695-6702(1996) [PubMed] [Europe PMC] [Abstract]
- "Identification and characterization of the human ortholog of rat STXBP1, a protein implicated in vesicle trafficking and neurotransmitter release."Genomics 48:373-376(1998) [PubMed] [Europe PMC] [Abstract]
- "DNA sequence and analysis of human chromosome 9." Nature 429:369-374(2004) [PubMed] [Europe PMC] [Abstract]
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
- "Ca2+-dependent phosphorylation of syntaxin-1A by the death-associated protein (DAP) kinase regulates its interaction with Munc18."J. Biol. Chem. 278:26265-26274(2003) [PubMed] [Europe PMC] [Abstract]
- "De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy."Nat. Genet. 40:782-788(2008) [PubMed] [Europe PMC] [Abstract]
- "A quantitative atlas of mitotic phosphorylation."Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed] [Europe PMC] [Abstract]
- "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
- "STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern." Epilepsia 51:2397-2405(2010) [PubMed] [Europe PMC] [Abstract]
- "Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations."Epilepsia 52:1828-1834(2011) [PubMed] [Europe PMC] [Abstract]
- "A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern."J. Child Neurol. 29:249-253(2014) [PubMed] [Europe PMC] [Abstract]
- "GABRA1 and STXBP1: novel genetic causes of Dravet syndrome." Neurology 82:1245-1253(2014) [PubMed] [Europe PMC] [Abstract]
- "A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype."NeuroReport 26:254-257(2015) [PubMed] [Europe PMC] [Abstract]